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Membranoproliferative Glomerulonephritis and Mixed Cryoglobulinemia as a Form of Presentation of Visceral Leishmaniasis.
Padrón Romero, Maite; Acevedo Ribó, Mercedes M; Ahijado Hormigos, Francisco Javier; Díaz Crespo, Francisco; Cueto Bravo, Laura; Herraiz Corredor, Cristina; Fernández Rojo, María Ángeles; Díaz-Tejeiro Izquierdo, Rafael.
Afiliação
  • Padrón Romero M; Department of Nephrology, Virgin Health Hospital, Toledo, Spain.
  • Acevedo Ribó MM; Department of Nephrology, Virgin Health Hospital, Toledo, Spain.
  • Ahijado Hormigos FJ; Department of Nephrology, Virgin Health Hospital, Toledo, Spain.
  • Díaz Crespo F; Department of Pathology, Virgin Health Hospital, Toledo, Spain.
  • Cueto Bravo L; Department of Nephrology, Virgin Health Hospital, Toledo, Spain.
  • Herraiz Corredor C; Department of Nephrology, Virgin Health Hospital, Toledo, Spain.
  • Fernández Rojo MÁ; Department of Nephrology, Virgin Health Hospital, Toledo, Spain.
  • Díaz-Tejeiro Izquierdo R; Department of Nephrology, Virgin Health Hospital, Toledo, Spain.
Am J Case Rep ; 21: e921445, 2020 May 27.
Article em En | MEDLINE | ID: mdl-32459796
ABSTRACT
BACKGROUND Visceral leishmaniasis (VL) is an endemic systemic disease in the Mediterranean countries, including Spain. This vector-borne infection can present with several clinical presentations, from asymptomatic to severe forms. Renal impairment is frequently described in VL but is usually mild and related to interstitial nephritis, being that glomerular involvement is rarely found. CASE REPORT We describe a case of a 69-year-old Spanish male presenting with subacute renal failure due to membranoproliferative glomerulonephritis and mixed cryoglobulinemia accompanied by other autoimmune features (hypocomplementemia, antinuclear and antiDNA antibodies). No hepatosplenomegaly was found with abdominal ultrasound. Hepatotropic viruses and human immunodeficiency virus serological markers were negatives. We initially suspect the presence of an autoimmune disease and the patient was treated with steroids without improvement. After an extensive study including renal and bone marrow biopsy, a correct diagnosis of visceral leishmaniasis was made, and treatment with liposomal amphotericin B was initiated, achieving renal function recovery and normalization of immunological manifestations. CONCLUSIONS Renal involvement can be an important feature of VL and it might be associated with increased morbidity and mortality. The association between mixed cryoglobulinemia and renal involvement in VL have rarely been described. VL is frequently associated with diverse autoimmune manifestations and it can be initially misdiagnosed, which could lead to fatal consequences. The role of the immune system in the formation of cryoglobulins are discussed. In our case, an autoimmune disease was initially suspected, and starting treatment with steroids pulses was initiated. However, the presence of mixed cryoglobulinemia in this patient who was hepatitis C serological marker negative and who had poor renal function recovery after immunosuppressive treatment made us suspect other pathologies. The presence of cryoglobulinemia with renal disease in endemic areas of Leishmania should make us exclude this infection before starting immunosuppressive treatment.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glomerulonefrite Membranoproliferativa / Crioglobulinemia / Insuficiência Renal / Leishmaniose Visceral Limite: Aged / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glomerulonefrite Membranoproliferativa / Crioglobulinemia / Insuficiência Renal / Leishmaniose Visceral Limite: Aged / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article